D-0004-2022 Class II Terminated
Recall Details
- Product Type
- Drugs
- Report Date
- October 13, 2021
- Initiation Date
- October 4, 2021
- Termination Date
- August 17, 2022
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 10,210 bottles
Product Description
Betaxolol Ophthalmic Solution, USP, 0.5%, (Betaxolol HCl 5.6 mg/mL), 5 mL dropper bottle, Rx only, Sterile, Manufactured by: Akorn, Inc., Lake Forest, IL 60045. Carton NDC: 17478-705-10, Bottle NDC 17478-705-11
Reason for Recall
Microbial Contamination of Sterile Products: Confirmed sterility failure identified during stability testing at the 12-month time point.
Distribution Pattern
Distributed Nationwide in the USA
Code Information
Lot 0B61A, Exp 01/31/2022